Fused heterocyclic compounds

a heterocyclic compound and compound technology, applied in the field of fused heterocyclic compounds, can solve the problems of lactic acidosis, a relatively serious side effect, and serious hypoglycemia that requires attention during use, and achieve the effect of peptidase in the report of these compounds

Inactive Publication Date: 2006-04-25
TAKEDA PHARMA CO LTD
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

While a sulfonylurea produce a potent hypoglycemic action, it sometimes causes serious hypoglycemia and requires attention during use.
A biguanide easily causes lactic

Method used

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  • Fused heterocyclic compounds
  • Fused heterocyclic compounds
  • Fused heterocyclic compounds

Examples

Experimental program
Comparison scheme
Effect test

example 1

3-(Aminomethyl)-4-butoxy-6-ethoxy-2-neopentyl-1(2H)-isoquinolinone hydrochloride

[0654](1) A solution of 4-fluorophthalic anhydride (8.31 g, 50 mmol) and ethyl 2-(neopentylamino)acetate (10.40 g, 60 mmol) in tetrahydrofuran (50 ml) was stirred at room temperature for 1 h. The reaction mixture was poured into water and extracted with ethyl acetate. The extract was washed with brine, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was dissolved in N,N-dimethylformamide (50 ml), and potassium carbonate (6.91 g, 50 mmol) and ethyl iodide (4.8 ml, 60 mmol) were added. The mixture was stirred at room temperature for 3 h. The reaction mixture was poured into water and extracted with ethyl acetate. The extract was washed with brine, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was dissolved in ethanol (50 ml) and 20% sodium ethoxide ethanol solution (34.04 g, 100 mmol) was added. The mixture was stirre...

example 2

3-(Aminomethyl)-4-butoxy-7-fluoro-2-neopentyl-1(2H)-isoquinolinone hydrochloride

[0672](1) To a solution of ethyl 7-fluoro-4-hydroxy-2-neopentyl-1-oxo-1,2-dihydro-3-isoquinolinecarboxylate (5.12 g, 31.9%) (from Example 1(1), 3.21 g, 10 mmol), 1-butanol (1.4 ml, 15 mmol) and tributylphosphine (5.0 ml, 20 mmol) in tetrahydrofuran (30 ml) was added 1,1′-(azodicarbonyl)dipiperidine (5.05. g, 20 mmol) and the mixture was stirred at room temperature for 3 h. The reaction mixture was concentrated, under reduced pressure and the residue was purified by silica gel column chromatography to give ethyl 4-butoxy-7-fluoro-2-neopentyl-1-oxo-1,2-dihydro-3-isoquinolinecarboxylate (3.55 g, 94.2%) as an oil.

[0673]1H-NMR(CDCl3) δ: 0.94 (9H, s), 1.01 (3H, t, J=7.1 Hz), 1.44 (3H, t, J=7.1 Hz), 1.51–1.63 (2H, m), 1.73–1.87 (2H, m), 3.95 (2H, t, J=6.4 Hz), 4.11 (2H, bs), 4.43 (2H, q, J=7.1 Hz), 7.40–7.50 (1H, m), 7.79 (1H, dd, J=5.2, 8.8 Hz), 8.09 (1H, dd, J=2.8, 9.4 Hz).

[0674](2) To a solution of 4-butoxy-...

example 3

3-(Aminomethyl)-4-butoxy-6-fluoro-2-neopentyl-1(2H)-isoquinolinone hydrochloride

[0686](1) To a solution of 4-butoxy-6-fluoro-3-hydroxymethyl-2-neopentyl-1(2H)-isoquinolinone (from Example 1(3), 1.68 g, 5 mmol) in tetrahydrofuran (10 ml) and toluene (10 ml) was added thionylchloride (0.73 ml, 10 mmol), and the resulting mixture was refluxed under heating for 2 h. The reaction mixture was poured into saturated aqueous sodium hydrogencarbonate solution and extracted with ethyl acetate. The extract was washed with brine, dried over anhydrous magnesium sulfate and concentrated under reduced pressure to give 4-butoxy-6-fluoro-3-chloromethyl-2-neopentyl-1(2H)-isoquinolinone (1.62 g, 92.0%) as an oil.

[0687]1H-NMR(CDCl3) δ: 0.98 (9H, s), 1.04 (3H, t, J=7.4 Hz), 1.51–1.69 (2H, m), 1.81–1.95 (2H, m), 3.94 (2H, t, J=6.6 Hz), 4.17 (2H, bs), 4.87 (2H, bs), 7.12–7.30 (1H, m), 7.35 (1H, dd, J=2.6, 9.6 Hz), 8.09 (1H, dd, J=5.8, 9.0 Hz).

[0688](2) A solution of 4-butoxy-6-fluoro-3-chloromethyl-2-neope...

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Abstract

The present invention provides a compound of the formula: wherein ring A is an optionally substituted 5 to 10-membered aromatic ring; R1 and R2 are the same or different and each is an optionally substituted hydrocarbon group or an optionally substituted heterocyclic group; X is a bond and the like; and L is a divalent hydrocarbon group, and a salt thereof, except 3-(aminomethyl)-2,6,7-trimethyl-4-phenyl-1(2H)-isoquinolinone, 3-(aminomethyl)-2-methyl-4-phenyl-1(2H)-isoquinolinone, 3-(aminomethyl)-6-chloro-2-methyl-4-phenyl-1(2H)-isoquinolinone and 3-(aminomethyl)-2-isopropyl-4-phenyl-1(2H)-isoquinolinone. The compound shows a superior peptidase-inhibitory activity and is useful as an agent for the prophylaxis or treatment of diabetes and the like.

Description

TECHNICAL FIELD[0001]The present invention relates to a novel fused heterocyclic compound having a peptidase (preferably dipeptidyl dipeptidase IV) inhibitory activity, which is useful as a prophylactic or therapeutic agent of diabetes and the like.BACKGROUND ART[0002]Peptidase is known to relate to various diseases. Dipeptidyl dipeptidase IV (hereinafter sometimes to be abbreviated as DPP-IV), which is one kind of peptidases, is serine protease that specifically binds with a peptide containing proline (or alanine) at the 2nd from the N terminal and cleaves the C-terminal side of the proline (or alanine) to produce dipeptide. DPP-IV has been shown to be the same molecule as CD26, and reported to be also involved in the immune system. While the role of DPP-IV in mammals has not been entirely clarified, it is considered to play an important role in the metabolism of neuropeptides, activation of T cells, adhesion of cancerous cells to endothelial cells, invasion of HIV into cells and t...

Claims

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Application Information

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IPC IPC(8): C07D217/02A61K31/47C07D217/24C07D217/26C07D401/04C07D401/06C07D401/12C07D405/06C07D413/04C07D417/04C07D417/06C07D495/04
CPCC07D217/24C07D217/26C07D401/04C07D401/06C07D495/04C07D405/06C07D413/04C07D417/04C07D417/06C07D401/12A61P5/48
Inventor OI, SATORUIKEDOU, KOJITAKEUCHI, KOJIOGINO, MASAKIBANNO, YOSHIHIROTAWADA, HIROYUKIYAMANE, TAIHEI
Owner TAKEDA PHARMA CO LTD
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